Incidental Mutation 'R1013:4930527J03Rik'
ID 95821
Institutional Source Beutler Lab
Gene Symbol 4930527J03Rik
Ensembl Gene ENSMUSG00000070489
Gene Name RIKEN cDNA 4930527J03 gene
Synonyms
MMRRC Submission 039117-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.293) question?
Stock # R1013 (G1)
Quality Score 109
Status Validated
Chromosome 1
Chromosomal Location 178103613-178104206 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) ACCC to ACC at 178276503 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000094270
Predicted Effect noncoding transcript
Transcript: ENSMUST00000192920
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.1%
  • 20x: 91.4%
Validation Efficiency 98% (39/40)
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700056E22Rik C T 1: 183,765,702 (GRCm39) S119N probably benign Het
Bclaf1 T A 10: 20,207,822 (GRCm39) probably benign Het
Bicdl2 A G 17: 23,884,377 (GRCm39) probably benign Het
C8a T C 4: 104,685,236 (GRCm39) I336V probably benign Het
Calcr A T 6: 3,692,621 (GRCm39) V374D probably damaging Het
Col28a1 A G 6: 7,999,452 (GRCm39) probably benign Het
Cuedc1 C T 11: 88,078,853 (GRCm39) A327V possibly damaging Het
Cul2 C A 18: 3,425,535 (GRCm39) Y378* probably null Het
Dnaaf10 A G 11: 17,178,183 (GRCm39) K226E probably damaging Het
Flt4 C T 11: 49,527,166 (GRCm39) probably benign Het
Gm8369 TG TGNG 19: 11,489,147 (GRCm39) probably null Het
Hivep1 A G 13: 42,310,438 (GRCm39) R893G probably damaging Het
Il10rb A G 16: 91,211,581 (GRCm39) N140D probably benign Het
Itga4 A G 2: 79,150,847 (GRCm39) M818V probably benign Het
Kyat3 T C 3: 142,432,007 (GRCm39) I245T probably damaging Het
Lck C T 4: 129,451,920 (GRCm39) C20Y probably damaging Het
Mcm6 T G 1: 128,276,778 (GRCm39) S271R probably benign Het
Megf10 A G 18: 57,394,291 (GRCm39) I472V probably benign Het
Mroh2a T C 1: 88,162,334 (GRCm39) probably null Het
Mrpl11 T C 19: 5,013,651 (GRCm39) I144T possibly damaging Het
Or2t26 G A 11: 49,039,977 (GRCm39) V298M probably damaging Het
Or8k25 G A 2: 86,244,319 (GRCm39) P26S possibly damaging Het
Pcdhb17 A G 18: 37,619,020 (GRCm39) D270G probably damaging Het
Plg G A 17: 12,597,608 (GRCm39) probably benign Het
Ppp3cb T A 14: 20,574,072 (GRCm39) E255D probably benign Het
Psenen A G 7: 30,261,802 (GRCm39) F38S possibly damaging Het
Rims4 C T 2: 163,705,849 (GRCm39) V262M possibly damaging Het
Sorl1 T C 9: 41,913,855 (GRCm39) N1358S probably benign Het
Trim3 G A 7: 105,267,102 (GRCm39) P426S probably benign Het
Ttc28 T C 5: 111,424,831 (GRCm39) M1552T probably benign Het
Unc13c T C 9: 73,840,614 (GRCm39) D79G probably benign Het
Zcchc14 A G 8: 122,333,664 (GRCm39) probably benign Het
Zfp354a T C 11: 50,951,677 (GRCm39) probably benign Het
Zfp729a T C 13: 67,767,626 (GRCm39) I868V probably benign Het
Other mutations in 4930527J03Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0294:4930527J03Rik UTSW 1 178,276,503 (GRCm38) exon noncoding transcript
R0323:4930527J03Rik UTSW 1 178,276,503 (GRCm38) exon noncoding transcript
R0392:4930527J03Rik UTSW 1 178,276,503 (GRCm38) exon noncoding transcript
R1247:4930527J03Rik UTSW 1 178,276,503 (GRCm38) exon noncoding transcript
R4804:4930527J03Rik UTSW 1 178,103,675 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- CCACCTGCTCAACAAAGCTGATTTC -3'
(R):5'- AGTGCTTCCTCCAGAACTAGGCTG -3'

Sequencing Primer
(F):5'- GAGAACTTGCCCTTCCTccg -3'
(R):5'- TCCAGAACTAGGCTGCTATTG -3'
Posted On 2014-01-05